Does COPPER Cause Post procedural haemorrhage? 106 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 106 reports of Post procedural haemorrhage have been filed in association with COPPER (Cuprum metallicum 7116). This represents 0.3% of all adverse event reports for COPPER.
106
Reports of Post procedural haemorrhage with COPPER
0.3%
of all COPPER reports
0
Deaths
3
Hospitalizations
How Dangerous Is Post procedural haemorrhage From COPPER?
Of the 106 reports, 3 (2.8%) required hospitalization, and 2 (1.9%) were considered life-threatening.
Is Post procedural haemorrhage Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for COPPER. However, 106 reports have been filed with the FAERS database.
What Other Side Effects Does COPPER Cause?
Device expulsion (11,141)
Device breakage (9,201)
Complication of device removal (7,895)
Foreign body in reproductive tract (7,050)
Device dislocation (6,955)
Complication of device insertion (6,078)
Pain (5,118)
Reproductive complication associated with device (3,654)
Embedded device (3,425)
Injury associated with device (2,895)
What Other Drugs Cause Post procedural haemorrhage?
LEVONORGESTREL (1,106)
RIVAROXABAN (930)
ASPIRIN (618)
APIXABAN (539)
ADALIMUMAB (476)
IBRUTINIB (269)
CLOPIDOGREL BISULFATE (235)
HEPARIN (174)
WARFARIN (170)
DABIGATRAN ETEXILATE (121)
Which COPPER Alternatives Have Lower Post procedural haemorrhage Risk?
COPPER vs CORDARONE
COPPER vs CORICIDIN HBP COLD AND FLU
COPPER vs CORTICOSTEROID NOS
COPPER vs CORTICOTROPIN
COPPER vs CORTISONE